Failure to find evidence for association between voltage-gated sodium channel gene SCN2A variants and febrile seizures in humans (Q74583039)

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11 November 2019

title

Failure to find evidence for association between voltage-gated sodium channel gene SCN2A variants and febrile seizures in humans (English)

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11 November 2019

author name string

Junko Nakayama

1

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11 November 2019

Nao Yamamoto

2

1 reference

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11 November 2019

Kenzo Hamano

3

1 reference

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11 November 2019

Nobuaki Iwasaki

4

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11 November 2019

Masayasu Ohta

5

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11 November 2019

Satoko Nakahara

6

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11 November 2019

Yumi Horigome

7

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11 November 2019

Chieko Nakahara

8

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11 November 2019

Emiko Noguchi

9

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11 November 2019

Junko Shiono

10

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11 November 2019

Yae Shimakura

11

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11 November 2019

Kimiko Yamakawa-Kobayashi

12

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11 November 2019

Akira Matsui

13

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11 November 2019

Tadao Arinami

14

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11 November 2019

publication date

1 August 2002

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11 November 2019

number of pages

3

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inferred from page(s)

published in

Neuroscience Letters

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11 November 2019

volume

329

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11 November 2019

issue

2

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11 November 2019

page(s)

249-251

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First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene

11 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2900651-1

7 January 2021

Genetic considerations in childhood epilepsy

1 reference

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7 January 2021

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

1 reference

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7 January 2021

The voltage-gated sodium channel gene SCN2A and idiopathic generalized epilepsy

1 reference

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7 January 2021

Evidence for a novel gene for familial febrile convulsions, FEB2, linked to chromosome 19p in an extended family from the Midwest

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2900651-1

7 January 2021

A gain-of-function mutation in the sodium channel gene Scn2a results in seizures and behavioral abnormalities

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2900651-1

7 January 2021

Identification of epilepsy genes in human and mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2900651-1

7 January 2021

Significant evidence for linkage of febrile seizures to chromosome 5q14-q15.

1 reference

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7 January 2021

A locus for febrile seizures (FEB3) maps to chromosome 2q23-24

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2900651-1

7 January 2021

Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes

1 reference

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7 January 2021

A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2900651-1

7 January 2021

Febrile convulsions in a national cohort followed up from birth. II--Medical history and intellectual ability at 5 years of age.

1 reference

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7 January 2021

Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2900651-1

7 January 2021

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2900651-1

1 reference

7 January 2021

10.1016/S0304-3940(02)00651-1

Identifiers

DOI

1 reference

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11 November 2019

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